Variant report

Variant	esv2625329
Chromosome Location	chr8:104382650-104384243
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:300)
CpG islands
(count:549)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:104384171-104384238	HepG2	liver:	n/a	n/a
2	BCL3	chr8:104382421-104382767	GM12878	blood:	n/a	chr8:104382716-104382725
3	BHLHE40	chr8:104383495-104383502	GM12878	blood:	n/a	n/a
4	CBX3	chr8:104383563-104383936	K562	blood:	n/a	n/a
5	CCNT2	chr8:104383433-104384203	K562	blood:	n/a	n/a
6	CEBPB	chr8:104382429-104382746	HepG2	liver:	n/a	chr8:104382600-104382613 chr8:104382601-104382612 chr8:104382600-104382611 chr8:104382600-104382611
7	CEBPB	chr8:104382276-104382708	K562	blood:	n/a	chr8:104382600-104382613 chr8:104382601-104382612 chr8:104382600-104382611 chr8:104382600-104382611
8	CHD2	chr8:104382540-104382712	K562	blood:	n/a	n/a
9	CHD2	chr8:104383405-104384099	K562	blood:	n/a	chr8:104383767-104383774
10	CHD2	chr8:104383806-104384112	HepG2	liver:	n/a	n/a
11	CTCF	chr8:104383380-104383530	GM12878	blood:	n/a	n/a
12	CTCF	chr8:104383400-104383550	A549	lung:	n/a	n/a
13	CTCF	chr8:104383974-104384041	GM13977	blood:	n/a	n/a
14	CTCF	chr8:104383360-104383510	HAc	cerebellar:	n/a	n/a
15	CTCF	chr8:104383400-104383550	K562	blood:	n/a	n/a
16	CTCF	chr8:104383400-104383550	GM12875	blood:	n/a	n/a
17	CTCF	chr8:104383420-104383570	AG09319	gingival:	n/a	n/a
18	CTCF	chr8:104383415-104383422	Fibrobl	skin:	n/a	n/a
19	CTCF	chr8:104383860-104384010	HepG2	liver:	n/a	n/a
20	CTCF	chr8:104383748-104383836	MCF-7	breast:	n/a	n/a
21	CTCF	chr8:104383967-104384069	MCF-7	breast:	n/a	n/a
22	CTCF	chr8:104383420-104383570	A549	lung:	n/a	n/a
23	CTCF	chr8:104382223-104382688	K562	blood:	n/a	n/a
24	CTCF	chr8:104383223-104384035	GM12878	blood:	n/a	n/a
25	CTCF	chr8:104383851-104384194	K562	blood:	n/a	n/a
26	CTCF	chr8:104383920-104384070	Caco-2	colon:	n/a	n/a
27	CTCF	chr8:104383400-104383550	BE2_C	brain:	n/a	n/a
28	CTCF	chr8:104383340-104383501	GM20000	blood:	n/a	n/a
29	CTCF	chr8:104383313-104383452	K562	blood:	n/a	n/a
30	CTCF	chr8:104383980-104384130	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr8:104383380-104383530	GM12867	blood:	n/a	n/a
32	CTCF	chr8:104383249-104383359	GM10248	blood:	n/a	n/a
33	CTCF	chr8:104383984-104384014	K562	blood:	n/a	n/a
34	CTCF	chr8:104383380-104383530	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr8:104383360-104383510	GM12873	blood:	n/a	n/a
36	CTCF	chr8:104383860-104384010	HCFaa	heart:	n/a	n/a
37	CTCF	chr8:104383400-104383550	GM12865	blood:	n/a	n/a
38	CTCF	chr8:104383400-104383550	GM06990	blood:	n/a	n/a
39	CTCF	chr8:104383260-104383570	MCF-7	breast:	n/a	n/a
40	CTCF	chr8:104383400-104383550	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr8:104383380-104383530	HCT-116	colon:	n/a	n/a
42	CTCF	chr8:104383942-104384017	ProgFib	skin:	n/a	n/a
43	CTCF	chr8:104383700-104383850	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr8:104383380-104383530	GM12868	blood:	n/a	n/a
45	CTCF	chr8:104383900-104384050	AG09319	gingival:	n/a	n/a
46	CTCF	chr8:104383852-104384153	K562	blood:	n/a	n/a
47	CTCF	chr8:104383400-104383550	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr8:104383400-104383550	GM12878	blood:	n/a	n/a
49	CTCF	chr8:104383400-104383550	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr8:104383400-104383550	HMEC	breast:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:104383433-104383483	HRE	kidney:	n/a
2	chr8:104383971-104384021	AoSMC	blood vessel:	n/a
3	chr8:104383413-104383463	HRCEpiC	kidney:	n/a
4	chr8:104383433-104383483	RPTEC	kidney:	n/a
5	chr8:104383715-104383765	PANC-1	pancreas:	n/a
6	chr8:104383730-104383780	MCF10A-Er-Src	breast:	n/a
7	chr8:104383730-104383780	HCF	heart:	n/a
8	chr8:104383724-104383774	HCPEpiC	choroid plexus:	n/a
9	chr8:104383413-104383463	ovcar-3	ovarian:	n/a
10	chr8:104383724-104383774	PrEC	prostate:	n/a
11	chr8:104383413-104383463	NH-A	brain:	n/a
12	chr8:104383433-104383483	U87	brain:	n/a
13	chr8:104383724-104383774	NHBE	bronchial:	n/a
14	chr8:104383722-104383772	HCF	heart:	n/a
15	chr8:104383730-104383780	HEEpiC	esophagus:	n/a
16	chr8:104383971-104384021	LNCaP	prostate:	n/a
17	chr8:104383499-104383549	HUVEC	blood vessel:	n/a
18	chr8:104383730-104383780	SK-N-MC	brain:	n/a
19	chr8:104383433-104383483	SAEC	small airway:	n/a
20	chr8:104383413-104383463	PrEC	prostate:	n/a
21	chr8:104383798-104383848	BJ	skin:	n/a
22	chr8:104383413-104383463	ProgFib	skin:	n/a
23	chr8:104383433-104383483	MCF10A-Er-Src	breast:	n/a
24	chr8:104383724-104383774	GM12892	blood:	n/a
25	chr8:104383798-104383848	A549	lung:	n/a
26	chr8:104383730-104383780	HMEC	breast:	n/a
27	chr8:104383433-104383483	HCF	heart:	n/a
28	chr8:104383413-104383463	AG09319	gingival:	n/a
29	chr8:104383499-104383549	HIPEpiC	eye:	n/a
30	chr8:104383433-104383483	PrEC	prostate:	n/a
31	chr8:104383971-104384021	HepG2	liver:	n/a
32	chr8:104383724-104383774	AG09309	skin:	n/a
33	chr8:104383730-104383780	U87	brain:	n/a
34	chr8:104383971-104384021	HIPEpiC	eye:	n/a
35	chr8:104383724-104383774	T-47D	breast:	n/a
36	chr8:104383798-104383848	SK-N-SH_RA	brain:	n/a
37	chr8:104383715-104383765	HCPEpiC	choroid plexus:	n/a
38	chr8:104383499-104383549	PFSK-1	brain:	n/a
39	chr8:104383798-104383848	AG09309	skin:	n/a
40	chr8:104383724-104383774	HUVEC	blood vessel:	n/a
41	chr8:104383724-104383774	HNPCEpiC	eye:	n/a
42	chr8:104383499-104383549	AG04450	lung:	fetal
43	chr8:104383413-104383463	AG10803	skin:	n/a
44	chr8:104383724-104383774	AG09319	gingival:	n/a
45	chr8:104383499-104383549	H1-hESC	embryonic stem cell:	embryo
46	chr8:104383724-104383774	PFSK-1	brain:	n/a
47	chr8:104383798-104383848	AG10803	skin:	n/a
48	chr8:104383798-104383848	HCPEpiC	choroid plexus:	n/a
49	chr8:104383499-104383549	BE2_C	brain:	n/a
50	chr8:104383730-104383780	HAEpiC	amniotic membrane:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:104382282..104385358-chr8:104387344..104390689,3	K562	blood:
2	chr8:104382288..104384118-chr8:104384150..104386828,2	MCF-7	breast:
3	chr8:104382634..104385222-chr8:104394415..104397249,2	K562	blood:
4	chr8:104383486..104387596-chr8:104393672..104397600,4	K562	blood:
5	chr8:104309661..104313454-chr8:104382208..104385836,8	MCF-7	breast:
6	chr8:104380544..104384762-chr8:104386449..104389451,3	K562	blood:
7	chr8:104309966..104312210-chr8:104383451..104386900,3	MCF-7	breast:
8	chr8:104291471..104292207-chr8:104382198..104383189,2	MCF-7	breast:
9	chr8:104383757..104385653-chr8:104425622..104427492,3	K562	blood:
10	chr8:104381633..104383715-chr8:104424202..104427564,3	K562	blood:
11	chr8:104382288..104384118-chr8:104384150..104386828,2	MCF-7	breast:
12	chr8:104382707..104385620-chr8:104427062..104430016,2	MCF-7	breast:
13	chr8:104382426..104384366-chr8:104426073..104428422,3	MCF-7	breast:

No data

Variant related genes	Relation type
CTHRC1	TF binding region
CTHRC1	CpG island
ENSG00000247081	chromatin interactions
ENSG00000207399	chromatin interactions
ENSG00000164934	chromatin interactions
ENSG00000164932	chromatin interactions
ENSG00000164930	chromatin interactions
ENSG00000164933	chromatin interactions
ENSG00000266289	chromatin interactions

Extended variants
information (count: 73 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:73 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549953055	chr8:104382699-104382700	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs570131493	chr8:104382715-104382716	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs373833211	chr8:104382739-104382740	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs571331947	chr8:104382770-104382771	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs202169210	chr8:104382784-104382785	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs550253842	chr8:104382795-104382796	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs568659165	chr8:104382803-104382804	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs576642597	chr8:104382820-104382821	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs377040928	chr8:104382909-104382910	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs36179117	chr8:104382910-104382911	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs183540627	chr8:104382911-104382912	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs535946793	chr8:104382915-104382916	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs554230468	chr8:104382916-104382917	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs62525535	chr8:104382917-104382918	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs62525536	chr8:104382970-104382971	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs62525537	chr8:104382978-104382979	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs62525538	chr8:104382992-104382993	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs62525539	chr8:104382997-104382998	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs201845082	chr8:104383027-104383028	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs529323406	chr8:104383029-104383030	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs375088999	chr8:104383039-104383040	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs62525540	chr8:104383059-104383060	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs62525541	chr8:104383067-104383068	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs62525542	chr8:104383073-104383074	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs62525543	chr8:104383084-104383085	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs200369071	chr8:104383087-104383088	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs62525544	chr8:104383088-104383089	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs62525545	chr8:104383124-104383125	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs111939848	chr8:104383131-104383132	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs62525546	chr8:104383144-104383145	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs62525547	chr8:104383149-104383150	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs200410403	chr8:104383152-104383153	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs113887327	chr8:104383174-104383175	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs561732316	chr8:104383190-104383191	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs6989245	chr8:104383217-104383218	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs6989247	chr8:104383219-104383220	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs7820626	chr8:104383315-104383316	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs534200107	chr8:104383333-104383334	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs559231938	chr8:104383353-104383354	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs186815658	chr8:104383375-104383376	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs541406150	chr8:104383376-104383377	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs7838990	chr8:104383425-104383426	Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs556795847	chr8:104383474-104383475	Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs574942938	chr8:104383475-104383476	Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs78898241	chr8:104383535-104383536	Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs374571201	chr8:104383564-104383565	Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs560258837	chr8:104383603-104383604	Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs527712648	chr8:104383626-104383627	Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs114456767	chr8:104383644-104383645	Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs116319535	chr8:104383647-104383648	Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Developmental delay	21147756	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104357800-104383400	Weak transcription	Aorta	Aorta
2	chr8:104377800-104383400	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr8:104378000-104383400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr8:104378000-104383400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr8:104381600-104383800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr8:104382400-104382800	Flanking Active TSS	K562	blood
7	chr8:104382400-104383400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:104382400-104383400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr8:104382600-104382800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
10	chr8:104382600-104382800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
11	chr8:104382600-104382800	Flanking Active TSS	A549	lung
12	chr8:104382600-104382800	Flanking Active TSS	HepG2	liver
13	chr8:104382600-104383400	Weak transcription	NH-A	brain
14	chr8:104382800-104383800	Active TSS	HepG2	liver
15	chr8:104382800-104384000	Active TSS	A549	lung
16	chr8:104382800-104384200	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr8:104382800-104384200	Active TSS	K562	blood
18	chr8:104383000-104384400	Weak transcription	Dnd41	blood
19	chr8:104383200-104383400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr8:104383200-104383400	Active TSS	Primary B cells from cord blood	blood
21	chr8:104383200-104383400	Bivalent/Poised TSS	Primary T cells fromperipheralblood	blood
22	chr8:104383200-104383400	Enhancers	Primary hematopoietic stem cells	blood
23	chr8:104383200-104383400	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr8:104383200-104383400	Bivalent/Poised TSS	Primary T helper cells PMA-I stimulated	--
25	chr8:104383200-104383400	Bivalent/Poised TSS	Primary T helper cells fromperipheralblood	blood
26	chr8:104383200-104383400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr8:104383200-104383400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr8:104383200-104383400	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr8:104383200-104383400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr8:104383200-104383400	Active TSS	Adipose Nuclei	Adipose
31	chr8:104383200-104383400	Active TSS	Fetal Stomach	stomach
32	chr8:104383200-104383400	Active TSS	Fetal Thymus	thymus
33	chr8:104383200-104383400	Enhancers	Right Ventricle	heart
34	chr8:104383200-104383400	Enhancers	HMEC	breast
35	chr8:104383200-104383600	Active TSS	Primary neutrophils fromperipheralblood	blood
36	chr8:104383200-104383800	Active TSS	HUES64 Cell Line	embryonic stem cell
37	chr8:104383200-104383800	Active TSS	Rectal Mucosa Donor 29	rectum
38	chr8:104383200-104384000	Active TSS	HUES6 Cell Line	embryonic stem cell
39	chr8:104383200-104384000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
40	chr8:104383200-104384000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr8:104383200-104384000	Bivalent/Poised TSS	Fetal Intestine Small	intestine
42	chr8:104383200-104384200	Active TSS	Primary T cells from cord blood	blood
43	chr8:104383200-104384200	Active TSS	Thymus	Thymus
44	chr8:104383200-104384400	Bivalent/Poised TSS	Fetal Brain Female	brain
45	chr8:104383200-104384400	Bivalent/Poised TSS	NHEK	skin
46	chr8:104383400-104383600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr8:104383400-104383600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
48	chr8:104383400-104383600	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
49	chr8:104383400-104383600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr8:104383400-104383600	Active TSS	Brain Hippocampus Middle	brain

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